Antibodies
Rat IgG2ab (subclass specific) goat polyclonal antibody, TRITC
| Applications | Can be used in Immunocytochemical and Immunohistochemical staining for the detection of IgG2 at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates; to identify and measure IgG2 in rat serum or other body fluids. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Working dilutions 1/20 - 1/80, depending on the method used. |
| Reactivities | Rat |
| Conjugation | TRITC |
Rat IgG2ab (subclass specific) goat polyclonal antibody, FITC
| Applications | Can be used to identify and measure IgG2, antigen or antibody, at the cellular and subcellular level by immunofluorescence staining of appropriately treated cell and tissue substrates, and to demonstrate circulating antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen or immune complex using a reference antibody of rat origin in the middle layer of the indirect test procedure. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Working dilutions: 1/20 - 1/80. |
| Reactivities | Rat |
| Conjugation | FITC |
Rat IgG2ab (subclass specific) goat polyclonal antibody, Azide Free
| Applications | As unlabelled primary or secondary reagent for indirect detection of IgG2a at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates; to prepare conjugates of the user’s own choice; to prepare an insoluble immunoaffinity adsorbent or a solid phase antibody reagent by coupling to an artificial carrier and as catching antibody in non-isotopic methodology and solid phase immunochemistry. When applied in any cytochemical or histochemical staining procedure or solid phase coupling technique, the optimum concentration of the IgG preparation should be established by titration before being used. Recommended working dilutions: Histochemistry: 1/100 - 1/250. ELISA and comparable non-precipitating antibody-binding assays: 1/500 - 1/5000. |
| Reactivities | Rat |
| Conjugation | Unconjugated |
Rat IgG2ab (subclass specific) goat polyclonal antibody, Biotin
| Applications | Can be used: In immunocytochemical and Immunohistochemical staining for the detection of IgG2 at the cellular and subcellular level of appropriately treated cell and tissue substrates. To demonstrate circulating IgG2 antibodies in serodiagnostic microbiology and autoimmune diseases. To identify a specific antigen using a reference antibody of Rat origin known to be of the IgG2 isotype in the middle layer of the indirect test procedure. In non-isotopic assay methodology (e.g. ELISA) to measure IgG2 in rat serum or other body fluids. As a second step an avidin or streptavidin conjugate of the user's choice has to be used. This immunoconjugate is not pre-diluted. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Recommended Working Dilutions: Histochemical and Cytochemical Use: 1/100-1/250. ELISA and comparable non-precipitating antibody-binding assays between: 1/2.000-1/10,000. |
| Reactivities | Rat |
| Conjugation | Biotin |
Rat IgG2b (subclass specific) goat polyclonal antibody, FITC
| Applications | Can be used to identify and measure IgG2b, antigen or antibody, at the cellular and subcellular level by immunofluorescence staining of appropriately treated cell and tissue substrates, and to demonstrate circulating antibodies in serodiagnostic microbiology and autoimmune diseases; to identify a specific antigen or immune complex using a reference antibody of rat origin in the middle layer of the indirect test procedure. This immunoconjugate is not pre-diluted. The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Recommended working dilutions: 1/20 - 1/80. |
| Reactivities | Rat |
| Conjugation | FITC |
Rat IgG2b (subclass specific) goat polyclonal antibody, Azide Free
| Applications | Can be used as unlabelled primary or secondary reagent for indirect detection of IgG2b at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates; to prepare conjugates of the user’s own choice; to prepare an insoluble immunoaffinity adsorbent or a solid phase antibody reagent by coupling to an artificial carrier and as catching antibody in non-isotopic methodology and solid phase immunochemistry. When applied in any cytochemical or histochemical staining procedure or solid phase coupling technique, the optimum concentration of the IgG preparation should be established by titration before being used. Recommended working dilutions: Histochemistry: 1/100 - 1/500. ELISA and comparable non-precipitating antibody-binding assays: 1/500 - 1/5000. |
| Reactivities | Rat |
| Conjugation | Unconjugated |
Rat IgE (Fc specific) goat polyclonal antibody, TRITC
| Applications | This antibody can be used: To identify and measure IgE, antigen or antibody, at the cellular and subcellular level by immunofluorescence staining of appropriately treated cell and tissue substrates. To identify circulating IgE antibodies in Rat serum or other body fluids. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Recommended Dilutions: 1/10-1/60. |
| Reactivities | Rat |
| Conjugation | TRITC |
Rat IgE (Fc specific) goat polyclonal antibody, FITC
| Applications | This antibody can be used In Immunocytochemical and Immunohistochemical staining for the detection of IgE at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates. To identify and measure IgE in Rat serum or other body fluids. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Recommended Dilutions: 1/20-1/80. |
| Reactivities | Rat |
| Conjugation | FITC |
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- Druggable Genome (386)
- Transmembrane (145)
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- Secreted Protein (31)
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- T cell receptor signaling pathway (11)
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- Chemokine signaling pathway (10)
- PPAR signaling pathway (10)
- Adipocytokine signaling pathway (9)
- Axon guidance (9)
- Colorectal cancer (9)
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- Insulin signaling pathway (9)
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- aspartate and glutamate metabolism (5)
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- Histidine metabolism (4)
- Long-term depression (4)
- Oxidative phosphorylation (4)
- Phenylalanine metabolism (4)
- Tyrosine metabolism (4)
- Vascular smooth muscle contraction (4)
- ABC transporters (3)
- Arachidonic acid metabolism (3)
- Butanoate metabolism (3)
- Dorso-ventral axis formation (3)
- Fatty acid metabolism (3)
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- GnRH signaling pathway (3)
- Hedgehog signaling pathway (3)
- Long-term potentiation (3)
- NOD-like receptor signaling pathway (3)
- Nucleotide excision repair (3)
- Progesterone-mediated oocyte maturation (3)
- RIG-I-like receptor signaling pathway (3)
- Renal cell carcinoma (3)
- Toll-like receptor signaling pathway (3)
- Type I diabetes mellitus (3)
- VEGF signaling pathway (3)
- mTOR signaling pathway (3)
- Allograft rejection (2)
- Asthma (2)
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- Base excision repair (2)
- Cardiac muscle contraction (2)
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- Glycerophospholipid metabolism (2)
- Glycine (2)
- Jak-STAT signaling pathway (2)
- Lysine degradation (2)
- N-Glycan biosynthesis (2)
- One carbon pool by folate (2)
- Pentose phosphate pathway (2)
- Phenylalanine (2)
- Propanoate metabolism (2)
- Purine metabolism (2)
- Regulation of autophagy (2)
- Systemic lupus erythematosus (2)
- Taste transduction (2)
- beta-Alanine metabolism (2)
- serine and threonine metabolism (2)
- tyrosine and tryptophan biosynthesis (2)
- Aminoacyl-tRNA biosynthesis (1)
- Ascorbate and aldarate metabolism (1)
- Autoimmune thyroid disease (1)
- Biosynthesis of unsaturated fatty acids (1)
- Circadian rhythm - mammal (1)
- D-Glutamine and D-glutamate metabolism (1)
- DNA replication (1)
- ECM-receptor interaction (1)
- Ether lipid metabolism (1)
- Graft-versus-host disease (1)
- Limonene and pinene degradation (1)
- Maturity onset diabetes of the young (1)
- Methane metabolism (1)
- Mismatch repair (1)
- Nitrogen metabolism (1)
- O-Glycan biosynthesis (1)
- Olfactory transduction (1)
- Phosphatidylinositol signaling system (1)
- Primary bile acid biosynthesis (1)
- Prion diseases (1)
- Renin-angiotensin system (1)
- Retinol metabolism (1)
- Riboflavin metabolism (1)
- Selenoamino acid metabolism (1)
- Sphingolipid metabolism (1)
- Taurine and hypotaurine metabolism (1)
- Valine (1)
- Viral myocarditis (1)
- leucine and isoleucine degradation (1)
